BMT CTN 2203 (Allogeneic Stem Cell Transplantation)

BMT CTN 2203 (Allogeneic Stem Cell Transplantation)

Es posible que algunos contenidos no estén disponibles en español.

Purpose of this Study

We are doing this study to find out if an experimental drug called ruxolitinib is a safe and effection option for preventing graft-versus-host disease when it is given in combination with the drugs tacrolimus and methotrexate before and after a peripheral blood stem cell transplant. We want to know if this study drug combination works better than the standard post-transplant treatment of cyclophosphamide, tacrolimus, and mycophenolate mofetil.

Who Can Participate?

Eligibility

Adults ages 18+ who will receive an allogeneic blood-forming stem cell transplant for one of the follow reasons:
  • Acute leukemia or chronic myelogenous leukemia with no circulating blasts and with less than 5% blasts in the bone marrow. Therapy related myeloid neoplasms are allowed.
  • Myelodysplasia/chronic myelomonocytic leukemia with no circulating blasts and with less than 10% blasts in the bone marrow (higher blast percentage allowed in MDS due to lack of differences in outcomes with < 5% versus 5-10% blasts in this disease). Therapy related myeloid neoplasms are allowed.
  • Lymphoma [follicular lymphoma, Hodgkin lymphoma, diffuse large B cell lymphoma, mantle cell lymphoma, peripheral T-cell lymphoma, angioimmunoblastic T-cell lymphoma and anaplastic large cell lymphoma]
For more information about this study, contact the study team at jennifer.tichon@duke.edu.

Age Range

18-110

Sex/Genders

Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No

What is Involved?

Description

If you choose to join this study, you will get a random assignment (like a coin flip) to either take part in Group A or Group B. If you are assigned to Group A, you will:
  • Take ruxolitinib twice a day as a pill by mouth beginning the day before your transplant. The dose given will be determined by the study's run-in phase. You will continue taking this drug for 12 months after your transplant.
  • Take tacrolimus as a pill by mouth each day or through your vein (IV) beginning 3 days before your transplant.
  • Take methotrexate through your vein on 3 different days (Days 1, 3, and 6) after your transplant.
If you are assigned to Group B, you will:
  • Take tacrolimus as a pill by mouth each day or through your vein (IV) beginning 3 days before your transplant.
  • Take mycophenolate mofetil through your vein or as a pill by mouth 3 times a day, beginning on Day 5 after your transplant. You will take this drug for 30 days.
  • Take cyclophosphamide through your vein on Days 3 and 4 after your transplant.
Your participation in the study will last about 2 years.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

Yes

Spanish Materials Available

No

Study Details

Full Title

A Randomized, Multicenter, Phase III Trial of Tacrolimus/Methotrexate/Ruxolitinib versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in
Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation

Principal Investigator

Sanghee
Hong

Protocol Number

PRO00117058

NCT ID

NCT06615050

Phase

III

Enrollment Status

Pending Open to Enrollment